Clinical Trials Regulatory Specialist
Tandem Clinical Research
Tandem Clinical Research is seeking a Regulatory Specialist to coordinate and maintain regulatory documentation across the lifecycle of clinical trials. This role supports study start-up, submissions, and ongoing documentation in collaboration with the Regulatory Manager, clinical teams, and sponsors. Responsibilities include preparing submissions to IRBs, maintaining ISFs and regulatory binders, and ensuring audit readiness. Strong knowledge of FDA regulations and ICH-GCP is essential. #J-18808-Ljbffr Tandem Clinical Research
Vacancy posted 5 days ago
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